1123-56-4

Basic information

• Product Name: 2,6-Dimethylbenzaldehyde
• Synonyms: 2,6-Dimethylbenzaldehyde 97%;2,6-DIMETHYLBENZALDEHYDE;m-Xylene-2-carboxaldehyde;2,6-Dimethylbenzaldehyde,97%;2-Formyl-m-xylene
• CAS NO: 1123-56-4
• Molecular Formula: C₉H₁₀O
• Molecular Weight: 134.18
• Product Categories: Aromatic Aldehydes & Derivatives (substituted);Aldehydes;C9;Carbonyl Compounds;Building Blocks;Carbonyl Compounds;Chemical Synthesis;Organic Building Blocks
• Mol File: 1123-56-4.mol
• Article Data: 33

Chemical Properties

• Melting Point: 27-30 °C(lit.)
• Boiling Point: 230 °C(lit.)
• Flash Point: 27 °C
• Appearance: White to yellow/Solid
• Density: 1.003 g/cm³
• Vapor Pressure: 0.122mmHg at 25°C
• Refractive Index: 1.5480
• Storage Temp.: Inert atmosphere,Room Temperature
• Water Solubility: Slightly soluble in water.
• Sensitive: Air Sensitive
• CAS DataBase Reference: 2,6-Dimethylbenzaldehyde(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-Dimethylbenzaldehyde(1123-56-4)
• EPA Substance Registry System: 2,6-Dimethylbenzaldehyde(1123-56-4)

Safety Data

• Hazard Codes: Xi
• Safety Statements: 24/25
• WGK Germany: 3
• Hazardous Substances Data: 1123-56-4(Hazardous Substances Data)

Usage

Chemical Properties

Colorless to yellow liquid or low melting solid

Uses

2,6-Dimethylbenzaldehyde has been used as a catalyst for steresopecific polymerization of propylene, and as well, has been used to study the control of postharvest botrytis fruit rot of strawberry and how the volatile Candida intermedia produced, effects mycelial growth of Botrytis cinerea.

InChI:InChI=1/C9H10O/c1-7-4-3-5-8(2)9(7)6-10/h3-6H,1-2H3

Upstream product

• 21900-37-8 2,6-dimethylbenzoyl chloride 
• 2039-90-9 2,6-dimethylstyrene 
• 529-20-4 2-methylphenyl aldehyde 
• 74-88-4 methyl iodide 
• 576-22-7 2-Bromo-m-xylene 
• 68-12-2 N,N-dimethyl-formamide 
• 6857-67-6 1,1,2,2-tetrakis-(2,6-dimethyl-phenyl)-ethane 
• 71-43-2 benzene 
• 64-18-6 formic acid 
• 608-28-6 2,6-dimethyliodobenzene 
• 15226-74-1 dicobalt octacarbonyl 
• 86364-02-5 2,6-dimethylphenyl trifluoromethanesulphonate 
• 576-26-1 2.6-dimethylphenol 
• 201230-82-2 carbon monoxide 

Downstream Products

• 93151-28-1 N,N-diethyl-N'-(2,6-dimethyl-benzyliden)-ethylenediamine 
• 93161-54-7 N,N-diethyl-N'-(2,6-dimethyl-benzylidene)-propanediyldiamine 
• 86347-16-2 4t-(2,6-dimethyl-phenyl)-but-3-en-2-one 
• 104292-54-8 5,10,15,20-tetrakis(2,6-dimethylphenyl)porphyrin 
• 63488-04-0 2-(2,6-Dimethylbenzyliden)-1,3-indandion 
• 527759-23-5 ethyl (E)-3-(2,6-dimethylphenyl)-2-propenoate 
• 67456-93-3 1,3-dimethyl-2-[(E)-2-phenyl-1-ethenyl]benzene 
• 927183-68-4 [1R,2S,(S)S]-1-(2,6-dimethyl)phenyl-2-methylthio-2-[2-(p-tolylsulfinyl)-phenyl]-1-ethanol 

Relevant articles and documents

Electrochromism of fast photochromic radical complexes forming light-unresponsive stable colored radical cation

We demonstrated the electrochromism of photochromic radical complexes containing triaryl imidazole: fast photoswitchable pentaarylbiimidazole (PABI) and the phenoxyl-imidazolyl radical complex (PIC). Cyclic voltammetry and spectroelectrochemistry revealed

Diels-Alder Cycloaddition of C60 with Photochemically Generated Hydroxy to o-quinodimethanes Governed by Steric Factors: A Mechanistic Study

Photoexcited o-alkyl-substituted benzaldehydes add to C60through their photoenol reactive intermediates producing stable [4 + 2] fullerene adducts. A mechanistic approach for this reactivity of C60 is provided, based mainly on intra-

An aerobic oxidation of alcohols into carbonyl synthons using bipyridyl-cinchona based palladium catalyst

We have reported an aerobic oxidation of primary and secondary alcohols to respective aldehydes and ketones using a bipyridyl-cinchona alkaloid based palladium catalytic system (PdAc-5) using oxygen at moderate pressure. ThePdAc-5catalyst was analysed using SEM, EDAX, and XPS analysis. The above catalytic system is used in experiments for different oxidation systems which include different solvents, additives, and bases which are cheap, robust, non-toxic, and commercially available on the industrial bench. The obtained products are quite appreciable in both yield and selectivity (70-85%). In addition, numerous important studies, such as comparisons with various commercial catalysts, solvent systems, mixture of solvents, and catalyst mole%, were conducted usingPdAc-5. The synthetic strategy of oxidation of alcohol into carbonyl compounds was well established and all the products were analysed using1H NMR,13CNMR and GC-mass analyses.

PROCESS FOR PREPARING 2,6-DIALKYLPHENYLACETIC ACIDS

The invention relates to a multi-stage process for preparing 2,6-dialkylphenylacetic acids of the general formula (I) by reacting 2,6-dialkylbromobenzenes with (1) magnesium, (2) a formamide, (3) an acid, (4) hydrogenation of the benzaldehyde obtained, (5

Palladium-Catalyzed Reductive Carbonylation of (Hetero) Aryl Halides and Triflates Using Cobalt Carbonyl as CO Source

An efficient protocol for the reductive carbonylation of (hetero) aryl halides and triflates under CO gas-free conditions using Pd/Co2(CO)8 and triethylsilane has been developed. The mild reaction conditions, enhanced chemoselectivity and, easy access to heterocyclic and vinyl carboxaldehydes highlights its importance in organic synthesis.